Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:31508369-31508516 | Common:4; Rare:61 | ||||
chr16:31873653-31873946 | Common:1; Rare:96 | ||||
chr16:46689134-46689317 | Common:1; Rare:72; Clinvar:2; Clinvar (benign):1 | ||||
chr16:46973555-46973781 | Rare:94 | ||||
chr16:47461016-47461356 | Common:2; Rare:128; Clinvar (benign):2 | ||||
chr16:48243966-48244360 | Common:3; Rare:95 | ||||
chr16:48385302-48385512 | Common:3; Rare:83 | ||||
chr16:50741708-50742162 | Common:7; Rare:135; Clinvar:1 | ||||
chr16:53703809-53704208 | Common:1; Rare:127; Clinvar:4; Clinvar (benign):2 | ||||
chr16:54286690-54286954 | Common:2; Rare:71 | ||||
chr16:55479037-55479207 | Rare:41 | ||||
chr16:56451280-56451605 | Common:1; Rare:104 | ||||
chr16:56519966-56520115 | Common:4; Rare:60; Clinvar:6; Clinvar (benign):5 | ||||
chr16:56608429-56608694 | Common:2; Rare:81 | ||||
chr16:56625525-56625854 | Common:1; Rare:99 |